MAUDE Adverse Event Report: MICROPORT ORTHOPEDICS INC. EVOLUTION MP CS INSERT SIZE 4+ 10MM RIGHT; KNEE COMPONENT

Model Number EIS4P10R

Device Problem Unstable (1667)

Patient Problem Failure of Implant (1924)

Event Type  Injury  

Manufacturer Narrative

This event will be updated once the investigation is complete.Trends will be evaluated.

Event Description

Allegedly, patient underwent right tkr on (b)(6) 2017.Base plate subsided into tibia resulting in significant valgus and instability.Patient revised on (b)(6) 2021 with evolution revision tibial base and stem extensions.Liner replaced with a 20mm one.(b)(6)- c1062.

• Brand Name: EVOLUTION MP CS INSERT SIZE 4+ 10MM RIGHT
• Type of Device: KNEE COMPONENT
• Manufacturer (Section D): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer (Section G): MICROPORT ORTHOPEDICS INC.; 5677 airline rd.; arlington TN 38002
• Manufacturer Contact: 5677 airline road; arlington, TN 38002 ; 9018674771
• MDR Report Key: 11467043
• MDR Text Key: 239359726
• Report Number: 3010536692-2021-00150
• Device Sequence Number: 1
• Product Code: HRY
• UDI-Device Identifier: M684EIS4P10R1
• UDI-Public: M684EIS4P10R1
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K093552
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 04/16/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Other
• Device Model Number: EIS4P10R
• Device Catalogue Number: EIS4P10R
• Device Lot Number: 1680390
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 02/21/2021
• Initial Date Manufacturer Received: 02/21/2021
• Initial Date FDA Received: 03/11/2021
• Supplement Dates Manufacturer Received: 02/21/2021
• Supplement Dates FDA Received: 04/16/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 77 YR